Because the genetic material of closely related pathogens are important pools from which novel genetic traits can be acquired, in this study, we investigated the occurrences of M protein (emm), superantigen genes, and streptolysin S structural gene (sagA), none of which had been demonstrated to exist in piscine isolates of GCSD. We also

analyzed the prevalence of the streptococcal pyrogenic exotoxin G gene (spegg) in piscine GCSD. Table 1 lists the 44 strains used in this study. The fish isolates of GCSD (n=30) investigated SAR245409 molecular weight in this study were obtained from clinical specimens of infected fish in Japan (yellowtail, amberjack and kingfish), Taiwan (mullet), and Malaysia (pompano and white spotted snapper), from the summer of 2002 find more to the end of 2007. Mammalian isolates of both the α-hemolytic GCSD (n=9) and the β-hemolytic Lancefield group C S. dysgalactiae ssp. equisimilis GCSE (n=5) collected from pigs with endocarditis were kindly provided by the Kumamoto Prefecture Meat Inspection Office in Japan. These isolates were also used for comparison. Stock cultures of GCSD and GCSE isolates were maintained in Todd–Hewitt broth (Difco, Sparks, MD) at −80 °C. All isolates

were routinely aerobically grown on Todd–Hewitt agar (THA; Difco) or blood agar (Columbia agar base; Becton Dickinson, Cockeysville, MD) containing 5% sheep blood (Nippon Bio-Test Laboratories, Japan), and incubated at 37 °C for 24 h. Lancefield serotyping C (Lancefield, 1933) was confirmed for GCSD and GCSE using Pastorex Strep (Bio-Rad, Marnes-la-Coquette, France). Genomic DNA was Interleukin-2 receptor extracted from bacterial colonies using DNAzol® reagent (Invitrogen, Carlsbad) according to the manufacturer’s protocol. To discriminate

fish isolates of GCSD from mammalian isolates of GCSD and GCSE, the specific PCR detection of fish isolates of GCSD using fish sodA gene primers has been performed according to the previously described method (Nomoto et al., 2008). Genomic DNA of GCSD fish isolates was screened by PCR for the presence of emm genes (Zhao et al., 2007), streptococcal pyrogenic exotoxin genes including speA, speB, speC (Hashikawa et al., 2004), speM, smeZ, ssa (Igwe et al., 2003), spegg, and sagA (Ikebe et al., 2004). This PCR assay was performed as described in the references. The primers used by Ikebe et al. (2004) for the amplification of spegg and sagA were designed to yield bands of 205 and 113 bp, respectively. Therefore, the sagA and spegg primers are redesigned for amplifying larger-size bands to examine these gene sequences. The primer pairs of sagaF (5′-TACTTCAAATATTTTAGCTACT-3′) and sagaR (5′-GATGATACCCCGATAAGGATAA-3′) for amplifying a 487-bp segment of sagA were designed based on the streptolysin S genes of S. dysgalactiae ssp. equisimilis (AY033399).